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Lenalidomide in patients with chemotherapy-induced polyneuropathy and relapsed or refractory multiple myeloma:
Chiara Briani1, Chiara Dalla Torre, Marta Campagnolo
1Department of Neurosciences, Neurological, Psychiatric, Sensorial, Reconstructive and Rehabilitative Sciences, University of Padova, Padova, Italy. chiara.briani@unipd.it
Abstract:
Lenalidomide, an immunomodulatory drug used in myeloma therapy, has been claimed to be less neurotoxic than thalidomide, but evidence is still weak. We prospectively assessed lenalidomide safety in myeloma patients to evaluate whether it would induce or modify a previously ensued chemotherapy-induced peripheral neuropathy (CIPN). Thirty consecutive patients (17 men, mean age 63.7 ± 9.4) previously treated with bortezomib and/or thalidomide and starting on lenalidomide (25 mg/day for 21-day cycles) for relapsed or refractory myeloma were assessed at baseline, 6, and 12 months from the beginning of lenalidomide with Total Neuropathy Score clinical version (TNSc), Eastern Cooperative Oncology Group (ECOG) performance status, and numeric rating scale (NRS) for pain. TNSc >2 was considered significant for CIPN. TNSc changes of at least 4 points from baseline value were considered clinically relevant. At baseline 16 of the 30 patients (53.3%) had CIPN (mean TNSc 5.8, range 3-15). After 6 months, 13 patients were unchanged, 1 improved, and 2 worsened. After 12 months the patient who had improved persisted stable, and the two who had worsened returned to TNSc baseline value. The 14 patients without CIPN at baseline did not develop neuropathy. NRS and ECOG performance status persisted unchanged. Our results demonstrate lenalidomide safety and very low neurotoxicity also in patients with pre-existing CIPN treated for 1 year.
Insights
Lenalidomide shows very low neurotoxicity in myeloma patients, even those with prior chemotherapy-induced peripheral neuropathy (CIPN). This immunomodulatory drug is safe for long-term use, with minimal impact on existing neuropathy.
Area of Science:
- Oncology
- Pharmacology
- Neurology
Background:
- Lenalidomide is an immunomodulatory drug used in multiple myeloma therapy.
- Evidence regarding lenalidomide's neurotoxicity compared to thalidomide is limited.
- Chemotherapy-induced peripheral neuropathy (CIPN) is a common concern in myeloma patients.
Purpose of the Study:
- To prospectively assess the safety and neurotoxicity of lenalidomide in multiple myeloma patients.
- To evaluate lenalidomide's effect on pre-existing chemotherapy-induced peripheral neuropathy (CIPN).
Main Methods:
- Prospective study of 30 consecutive myeloma patients starting lenalidomide.
- Assessment using Total Neuropathy Score clinical version (TNSc), ECOG performance status, and NRS for pain at baseline, 6, and 12 months.
- CIPN defined as TNSc >2; clinically relevant change as >=4 points from baseline.
Main Results:
- At baseline, 53.3% of patients had pre-existing CIPN (mean TNSc 5.8).
- After 12 months, no new cases of significant neuropathy developed, and existing CIPN remained stable or improved.
- Numeric Rating Scale (NRS) for pain and ECOG performance status remained unchanged throughout the study.
Conclusions:
- Lenalidomide demonstrates a favorable safety profile with very low neurotoxicity in multiple myeloma patients.
- The drug is safe for patients with pre-existing CIPN, with no significant worsening observed over one year.
- Lenalidomide can be considered a safe therapeutic option for relapsed or refractory myeloma, even in patients with prior neuropathy.
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